Expression of nonclassical molecule human leukocyte antigen–G in oral lesions
Abstract Introduction Human leukocyte antigen (HLA)–G is a nonclassic class I molecule that acts as a modulator of immune responses, and the expression of these molecules in virus-infected cells has been associated with subversion of the immune response. Objective In this study, we performed a cross...
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Veröffentlicht in: | American journal of otolaryngology 2012-03, Vol.33 (2), p.193-198 |
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Sprache: | eng |
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Zusammenfassung: | Abstract Introduction Human leukocyte antigen (HLA)–G is a nonclassic class I molecule that acts as a modulator of immune responses, and the expression of these molecules in virus-infected cells has been associated with subversion of the immune response. Objective In this study, we performed a cross-sectional study, systematically comparing the expression of the HLA-G in benign, premalignant, and malignant oral lesions and correlating it with the presence of high-risk and low-risk human papillomavirus (HPV) types. Specimens and Methods Oral biopsies were collected from 51 patients and analyzed by immunohistochemistry using anti–HLA-G antibody. Human papillomavirus detection and typing from oral biopsies were obtained by polymerase chain reaction using GP5+/GP6+ and specific primers. Results The 51 biopsies were stratified into 3 groups according to lesion grade: oral benign lesions (oral hyperplasia and papilloma, n = 16), oral premalignant lesions (oral leukoplakia with dysplasia and lichen planus, n = 17), and malignant lesions (oral squamous cell carcinoma, n = 18). Human leukocyte antigen–G overexpression was mainly observed in benign and premalignant oral lesions but was not related to HPV infection ( P > .05). On the other hand, HPV DNA was detected in 24 (47%) oral lesions, mainly in benign and premalignant lesions, with the most frequent type detected being high-risk HPV type. Conclusion The HLA-G molecule was expressed in a significant number of benign oral lesions and was not correlated with HPV infection or oral cancer. |
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ISSN: | 0196-0709 1532-818X |
DOI: | 10.1016/j.amjoto.2010.08.001 |